Description
This panel was developed and is maintained by VCGS.

1 reviewer

  • Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

7 Entities

7 reviewed, 5 green

List Entity Reviews Mode of inheritance Details
7 Entitiess
Green Green List (high evidence)
AGPS
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Rhizomelic chondrodysplasia punctata, type 3, MIM# 600121
Tags
Green Green List (high evidence)
ARSE
1 review
1 green
X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Chondrodysplasia punctata, X-linked recessive, MIM# 302950
Tags
  • new gene name
Green Green List (high evidence)
EBP
1 review
1 green
X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Chondrodysplasia punctata, X-linked dominant, MIM# 302960
Tags
Green Green List (high evidence)
GNPAT
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Rhizomelic chondrodysplasia punctata, type 2, MIM# 222765
  • MONDO:0009112
Tags
Green Green List (high evidence)
PEX7
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Rhizomelic chondrodysplasia punctata, type 1, MIM# 215100
  • MONDO:0008972
Tags
Amber Amber List (moderate evidence)
C16orf62
1 review
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert list
  • Expert Review Amber
Phenotypes
  • Ritscher-Schinzel syndrome-3 (RTSC3), MIM#619135
Tags
Amber Amber List (moderate evidence)
PEX5
1 review
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review
  • Expert Review Amber
Phenotypes
  • Rhizomelic chondrodysplasia punctata, type 5, MIM# 616716
  • MONDO:0014743
Tags

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